Diagnostic accuracy of small-for-gestational-age status for infant mortality and school-age outcomes of live births <28 weeks’ gestation: a cohort study

医学 小于胎龄 胎龄 妊娠期 婴儿死亡率 人口学 队列 产科 队列研究 怀孕 人口 内科学 环境卫生 社会学 遗传学 生物
作者
Lex W. Doyle,Julie Chen,Rosemarie A. Boland,Stefan C. Kane,Rheanna Mainzer,Gehan Roberts,Elisha K. Josev,Marissa Clark,Peter J. Anderson,Jeanie L.Y. Cheong
出处
期刊:Archives of Disease in Childhood-fetal and Neonatal Edition [BMJ]
卷期号:108 (6): 649-654 被引量:1
标识
DOI:10.1136/archdischild-2023-325515
摘要

To determine the diagnostic accuracy of small-for-gestational-age (SGA; <10th centile) status for infant mortality and adverse school-age outcomes in infants born extremely preterm (EP; <28 weeks' gestation).Geographical cohort studies.The state of Victoria, Australia.For mortality, live births 22-27 weeks' gestation from 2009 to 2017 offered active care after birth. For school-age outcomes, survivors to 8 years' corrected age born in 1991-1992, 1997 or 2005.SGA <10th centile on four commonly used growth references: three derived from neonatal data (Fenton, UK-WHO and Intergrowth Newborn Size) and one from fetal data (Intergrowth Estimated Fetal Weight).(a) Infant mortality; (b) major neurodevelopmental disability, and poor performance on tests of IQ, academic achievement, motor function, and executive function.Infant mortality data were available for 2040 infants, and neurodevelopmental data for 499 children. Diagnostic accuracy of SGA status was low overall and varied with the growth reference. Positive predictive values for infant mortality ranged from 18% to 21%, only marginally higher than its 18% prevalence. Compared with a prevalence of 17%, positive predictive values for major neurodevelopmental disability ranged from 30% to 38% for the neonatal growth references but was only 20% for Intergrowth Estimated Fetal Weight. SGA status was also associated with lower IQ, poor academic achievement and poor motor performance.Among infants born EP, the diagnostic accuracy of SGA status was low for both infant mortality and adverse neurodevelopmental outcomes at school age, but importantly varied with the growth reference used to identify SGA status.
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